Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Bloating - Help? :(


Waitingindreams

Recommended Posts

w8in4dave Community Regular

Good Luck let us know how it all goes! 


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



KMMO320 Contributor

I know some people experience major bloating after eating foods with gluten in them...but I have been bloated almost non stop, even after cutting gluten out of my diet. 

 

My stomach is huge, I have no idea why the bloating won't go down. I am pretty careful, even going so far as to eliminate hand sanitizers and shampoos with gluten in them. I read that digestive supplements and probiotics as well as drinking more water can help the bloat go down. Does anyone else have any other tips? For awhile I couldn't drink much water...it was making me sick..but now I am gradually able to drink more water again, thankfully. Can anyone recommend good probiotics/digestive enzymes that actually work for bloating? It seems like there's always something wrong. I know my stomach is far too big for my size...it looks like I'm pregnant.. please help? :(

 

I also have gall stones, not sure if that matters...

 

I am a little under a year and a half gluten free now. Only recently have I discovered horrible bloating, gas and pain after eating large amounts of dairy. I seem to be ok with a yogurt here and there, a little cheese and half and half in my coffee. But if I eat a bowl of ice cream, or gluten-free Mac and Cheese, gluten-free pizza....I get very bloated. 

last night, I had ice cream and I was so bloated, gassy and sick to my stomach that I just went right to bed. Every so often I try to eat it, with the same results. I guess I should just give up. I was actually ok going Gluten Free, it was very non-eventful and I don't have cravings. But cutting Dairy hurts. 

bartfull Rising Star

There are non-dairy ice creams available at your health food store. One of them is made with coconut "cream". I've never tried it but a friend of mine has and she loved it. :)

GFinDC Veteran

There are non-dairy ice creams available at your health food store. One of them is made with coconut "cream". I've never tried it but a friend of mine has and she loved it. :)

 

I think the coconut ice cream brand is called "So Delicious".  There are also gelato's and ices available as an alternative to dairy based stuff.

  • 2 months later...
Waitingindreams Enthusiast

Hi all!

 

The non dairy ice cream "So Delicious" (made with coconut milk - though they have a soy variety as well) IS very good! I got off the SCD diet when frustrated with it - but I have gone lactose free and mostly dairy free, apart from my almond cheese (no lactose, but has casein) I noticed that yeast seems to trigger GI symptoms..(bloating, "the big D") AND it seemed to make my skin issues worse...so I am off yeast as well. 

 

The bloating comes and goes. :( I never noticed my stomach so big as it was when my primary care doctor told me to try Gas-x for the bloat. It MADE me gassy, (which I took as a good sign, I thought it was kind of cleansing all of the gas out?) and then when I looked in the mirror I wanted to cry. My stomach was HUGE. HUGGGEE. Needless to say, I never touched those pills again. 

 

I think my bloating has to do with the lactose intolerance, the yeast issue, and I also just found out I have abdominal hernia (per my naturopathic doctor) but he says there are non surgical methods to treat that. I bet that is a good source of why I am bloated. (I'm very 'tender' and sore when the doctors push down on my stomach, and it feels kind of hard) So I'm guessing that once the hernia is corrected, the bloating will get better. I am not as consistently bloated as I once was, which is a good sign! I've also been advised to try digestive enzymes called Vitalzyme..anyone have luck with these? They claim to help digest gluten (and also casein)...not that I would ever intentionally eat gluten, but I wonder if it helps with CC issues? 

w8in4dave Community Regular

Hi all!

 

The non dairy ice cream "So Delicious" (made with coconut milk - though they have a soy variety as well) IS very good! I got off the SCD diet when frustrated with it - but I have gone lactose free and mostly dairy free, apart from my almond cheese (no lactose, but has casein) I noticed that yeast seems to trigger GI symptoms..(bloating, "the big D") AND it seemed to make my skin issues worse...so I am off yeast as well. 

 

The bloating comes and goes. :( I never noticed my stomach so big as it was when my primary care doctor told me to try Gas-x for the bloat. It MADE me gassy, (which I took as a good sign, I thought it was kind of cleansing all of the gas out?) and then when I looked in the mirror I wanted to cry. My stomach was HUGE. HUGGGEE. Needless to say, I never touched those pills again. 

 

I think my bloating has to do with the lactose intolerance, the yeast issue, and I also just found out I have abdominal hernia (per my naturopathic doctor) but he says there are non surgical methods to treat that. I bet that is a good source of why I am bloated. (I'm very 'tender' and sore when the doctors push down on my stomach, and it feels kind of hard) So I'm guessing that once the hernia is corrected, the bloating will get better. I am not as consistently bloated as I once was, which is a good sign! I've also been advised to try digestive enzymes called Vitalzyme..anyone have luck with these? They claim to help digest gluten (and also casein)...not that I would ever intentionally eat gluten, but I wonder if it helps with CC issues? 

I just want to say. I have found out Soy is a problem with me. Evidently Soy is very CC'd with Gluten because of the equipment shared. I was CC'd with it a few months ago. You may want to look into that. It is so hard to figure all this out! After a while (It depends on the person) you may be able to get Lactose and corn and stuff back. I am afraid I will not get Soy back. I guess it depends on the person. 

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,952
    • Most Online (within 30 mins)
      7,748

    SY8
    Newest Member
    SY8
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.